Associate Director, Biostatistics

Associate Director, Biostatistics

Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics Associate Director, Biostatistics The Associate Director of Biostatistics will be responsible for leading the execution of statistical components of Corcept Development programs. This position will manage external statisticians and statistical programmers.

This is a hybrid role typically requiring on-site presence at least 3 days per week.

Responsibilities: Partner with Clinical Development, Regulatory, Manufacturing, and Commercial organizations on the design and execution of clinical trials in the Corcept portfolio

Oversee execution of the statistical components of clinical studies by CROs and independent contractors. Manage on-time and quality delivery of CRO-generated analyses results

Partner with Statistical Programming in generation of statistical analyses for internal and external presentations, and validation statistical analyses results generated by CROs

Partner with Statistical Programming in the evaluation of CDISC electronic data packages for completeness, regulatory standards compliance, and submission readiness

Stay current with regulatory requirements for statistical methods of analyses and scientific developments in statistical methods for clinical trials

Consult internal audit team in assessing regulatory compliance of CROs with respect to statistical SOPs

Participate in standards governance and development of Corcept Biostatistical SOPs

Preferred Skills, Qualifications, and Technical Proficiencies:

Knowledge of global regulatory guidance on statistical methods for analyses of clinical data, and global submission requirements

Proficiency with statistical programming in SAS. Familiarity with SAS/GRAPH, SAS/MACRO, and R

Demonstrated ability to apply complex statistical methods, conduct and interpret the results

Preferred Education and Experience: D. in Statistics, Biostatistics, or Mathematics

5+ years of experience in clinical trial development

Demonstrated ability for project management of projects in clinical development

Experience managing delivery of statistical projects by CROs

The pay range that the Company reasonably expects to pay for this headquarters-based position is $183,500 – $269,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

Corcept Therapeutics is hiring for this role on CareerPlace.

Apply on the company website through Corcept Therapeutics.

Imported from employer careers page. Source ref: e71ab7b5b81d.